Naked d-orbital in a centrochiral Ni(II) complex as a catalyst for asymmetric [3+2] cycloaddition

作者：Sohtome Yoshihiro^*; Nakamura Genta; Muranaka Atsuya; Hashizume Daisuke^*; Lectard Sylvain; Tsuchimoto Teruhisa; Uchiyama Masanobu; Sodeoka Mikiko^*

来源：Nature Communications, 2017, 8(1): 14875.

DOI：10.1038/ncomms14875

Chiral metal catalysts have been widely applied to asymmetric transformations. However, the electronic structure of the catalyst and how it contributes to the activation of the substrate is seldom investigated. Here, we report an empirical approach for providing insights into the catalytic activation process in the distorted Ni(II)-catalysed asymmetric [3+2] cycloaddition of alpha-ketoesters. We quantitatively characterize the bonding nature of the catalyst by means of electron density distribution analysis, showing that the distortion around the Ni(II) centre makes the dz(2) orbital partially 'naked', wherein the labile acetate ligand is coordinated with electrostatic interaction. The electron-deficient dz(2) orbital and the acetate act together to deprotonate the alpha-ketoester, generating the (Lambda)-Ni(II)-enolate. The solid and solution state analyses, together with theoretical calculations, strongly link the electronic structure of the centrochiral octahedral Ni(II) complex and its catalytic activity, depicting a cooperative mechanism of enolate binding and outer sphere hydrogen-bonding activation.

• 出版日期2017-4-6